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Recalls affecting Michigan

Data last updated: September 8, 2026 at 1:13 PM UTC

17,010 recalls found

Just announced

Straight from FDA press releases — not yet formally classified or risk-graded
UnclassifiedUndeclaredAnnounced September 4, 2026

Business Pill, Branch Manager for Men — dietary supplements marketed for male sexual enhancement

Products contain undeclared yohimbine

▸Full report
Dietary SupplementsFood & Beverages

Recalling firm: SUPPLX.com

Grant-Valkaria, Florida - SUPPLX.com is voluntarily recalling Business Pill and Branch Manager for Men, products marketed as dietary supplements for male sexual enhancement, because FDA laboratory analysis confirmed that both products contain yohimbine that is not declared on the product labels.

Company contact: (321) 341-9501 · SupplxRecall@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 4, 2026

Foods Alive — Moringa Leaf Powder

Potential to be contaminated with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Foods Alive Inc.

Foods Alive Inc of Angola, IN, is recalling its 8-ounce packages of organic moringa leaf powder because they have the potential to be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

B. Braun — 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container

Presence of particulate matter identified as iron oxide

▸Full report
Drugs

Recalling firm: B. Braun Medical Inc.

“On September 3, 2026 firm updated their press release to include additional contaminants.” FOR IMMEDIATE RELEASE – September 3, 2026– Bethlehem, PA, B. Braun Medical Inc (B. Braun) is voluntarily recalling three (3) lots of 0.9% Sodium Chloride Injection USP, 100 mL, in a 150 mL PAB® Container, to the hospital/healthcare facility/user level due to presence of particulate matter identified as iron…

Company contact: recalls@bbraunusa.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced September 3, 2026

Great Value — Organic Triple Berry Blend

Possible E. Coli Contamination

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Frutas y Hortalizas del Sur S.A.

September 02, 2026. Frutas y Hortalizas del Sur S.A., San Carlos, Chile expands its July 3, 2026, recall of frozen organic IQF blueberries to include one lot of Great Value frozen Organic Triple Berry Blend 10 OZ because of potential contamination with Escherichia coli O145:H28 (E. coli O145) .

Company contact: Info.foodsafety@comfrut.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced September 3, 2026

American Regent, Inc. — Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vial

Presence of particulate matter and lack of sterility assurance

▸Full report
Food & Beverages

Recalling firm: American Regent, Inc.

FOR IMMEDIATE RELEASE – September 3, 2026 – New Albany, OH, American Regent, Inc. is conducting a nationwide voluntary recall of three lots of Epinephrine Injection, USP 30 mg/ 30 mL (1 mg/mL) multi dose vials to the consumer level. Customer complaints were received for leaking and cracked vials, resulting in lack of assurance of sterility.

View FDA’s announcement (opens in a new tab)
UnclassifiedUndeclaredAnnounced August 31, 2026

Lipofit — Lipofit Extreme 2.0 Fat Burner Dietary Supplement

Undeclared Fluoxetine and 2,4-Dinitrophenol (DNP)

▸Full report
Dietary SupplementsDrugs

Recalling firm: Ana Salazar Modela Tu Cuerpo Inc.

FOR IMMEDIATE RELEASE - August 27, 2026 - Davie, Florida – Ana Salazar Modela Tu Cuerpo Inc. is recalling Lipofit Extreme Fat Burner 2.0, Lot 25M12F, expiration date 09/2027, to the consumer level.

Company contact: (954) 305-1004 · yandrydy@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedAnnounced August 31, 2026

Kofinas — Garlic Mediterranean Infused Extra Virgin Olive Oil 500 ml, 250 ml, and 100 ml

Contains garlic essential oil not approved for culinary use

▸Full report
Food & BeveragesIngredients

Recalling firm: LMSI LLC

Cincinnati, OH (Aug. 29, 2026) - LMSI LLC/ Kofinas Olive Oil is issuing a voluntary recall of its Garlic Mediterranean infused extra virgin olive oil for using a garlic essential oil not approved for culinary use. The flavored oil was bottled in glass bottles in 500 ml, 250 ml, and 100 ml sizes.

View FDA’s announcement (opens in a new tab)
UnclassifiedAllergenUndeclaredAnnounced August 31, 2026

Little Temptations — Chocolatey Eyeballs, 7 oz., 10 oz., 10.5 oz., 11 oz., and 16 oz.

Undeclared milk

▸Full report
Food & BeveragesAllergens

Recalling firm: Crystal Temptations

Crystal Temptations of North Arlington, NJ is recalling Halloween Chocolatey Eyeballs because they contain undeclared MILK allergens. People who have an allergy or severe sensitivity to milk run the risk of serious or life-threatening allergic reaction if they consume these products.

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Everything Sprouts — Robust Radish Mix, 5oz Cups

Potential to be contaminated with Shiga toxin-producing Escherichia coli (STEC) or Salmonella.

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Everything Sprouts, LLC

Everything Sprouts, LLC, based in Minneapolis, MN is expanding its voluntary recall of sprouts to include certain lots of Robust Radish Sprout Mix because it has the potential to be contaminated with Shiga toxin producing Escherichia coli (STEC) or Salmonella bacteria.

Company contact: everythingsproutsmn@gmail.com

View FDA’s announcement (opens in a new tab)
UnclassifiedBacteria/virusAnnounced August 29, 2026

Martina — Mangoes

Potential contamination with Salmonella

▸Full report
Food & BeveragesFoodborne Illness

Recalling firm: Panorama Produce

MAMARONECK, NY, AUG. 28, 2026 - Panorama Produce is recalling 302 boxes of size 9 (nine) mangoes because they may be contaminated with Salmonella , an organism which can cause serious and sometimes fatal infections in young children, frail or elderly people, and others with weakened immune systems.

Company contact: information@panoramaproduce.com

View FDA’s announcement (opens in a new tab)
NewestOldest
High riskLow riskAll
Wording
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

Waffles packaged as follows: a) Aunt Jemima(R) Waffles, 144 COUNT, NET WT 7.88 LBS, UPC 001960043575 b) Aunt Jemima(R) Jumbo Square Waffles, 144 COUNT, NET WT 11.4 LBS, UPC 001960043573 c) Aunt Jemima(R) Waffles, 144 COUNT, NET WT 7.88 LBS, UPC 001960043575 d) Mrs. Butter-worth's(R) WAFFLES, 72 COUNT, NET WT 7.88 LBS, UPC 001960046009 e) Mrs. Butter-worth's(R) WAFFLES, 144 COUNT, NET WT 11.4 LBS, UPC 001960046001 f) Hilltop HEARTH WAFFLES, 18 BOLSAS CON 8 PIEZAS, PESO NETO 11 LBS 6.9 OZ, UPC 075810861817 g) Aunt Jemima(R) Original Round Waffles, 144 COUNT, NET WT 11.25 LBS, UPC 001960043580

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2313-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 12 OATMEAL PANCAKES, NET WT 14.8oz UPC 019600064909

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2296-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 14 LOW FAT WAFFLES, NET WT 17.18oz UPC 019600062301

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2306-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) CINNAMON FRENCH TOAST, 6 COUNT, NET WT 12.5oz, UPC 019600058908

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2301-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 12 PANCAKES MADE WITH WHOLE GRAIN, NET WT 14.5oz UPC 019600066408

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2297-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

Aunt Jemima(R) Original Thin French toast, 144 COUNT, NET WT 13.5 LBS, UPC 001960005870

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2311-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 12 BLUEBERRY PANCAKES, NET WT 14.8oz UPC 019600064701

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2295-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

Hilltop HEARTH WAFFLES, 18 BOLSAS CON 8 PIEZAS, PESO NETO 11LB 6.4 oz, UPC075810843855

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2316-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

Homestyle pancakes packaged as follows: a) AUNT JEMIMA(R) 12 HOMESTYLE PANCAKES, NET WT 14.8oz UPC 019600069102 b) AUNT JEMIMA(R) HOMESTYLE PANCAKES, 60 COUNT, NET WT 4.63 LBS, UPC 019600435907 c) AUNT JEMIMA(R) HOMESTYLE PANCAKES,60 COUNT (MEXICO), NET WT 4.29 LBS, UPC 019600435921 d) AUNT JEMIMA(R) HOMESTYLE PANCAKES, 60 COUNT, NET WT 4.29 LBS, UPC 001960043596

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2299-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 14 BUTTERMILK WAFFLES, NET WT 17.18oz UPC 019600062103

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2304-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) MiNi pancakes, CINNAMON ROLL, NET WT 3.2 OZ, UPC 001960043568

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2309-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) LIL' GRIDDLES(TM) BLUEBERRY MINI PANCAKES, 40 COUNT, NET WT 14.5oz UPC 019600054603

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2292-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) MiNi pancakes, MAPLE BLAST, NET WT 3.2 OZ, UPC 001960043563

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2307-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) 14 HOMESTYLE WAFFLES, NET WT 17.18oz UPC 019600062004

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2303-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

Mrs. Butter-worth's(R) ORIGINAL PANCAKES, 144 COUNT, NET WT 10.6 LBS, UPC 001960046004

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2318-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

French toast packaged as follows: a) Hilltop HEARTH, FRENCH TOAST, 18 8 COUNT BAGS, NET WT 10 LB 11.2 OZ, UPC 075810861816 b) Hilltop HEARTH, FRENCH TOAST, 12 6 COUNT BAGS, NET WT 10 LB 11.2 OZ, UPC 075810843855 c) Hilltop HEARTH FRENCH TOAST, 12 6 COUNT BAGS, NET WT. 10 LB 11.2 OZ, UPC 075810843854 d) Mrs. Butter-worth's(R), FRENCH TOAST, 144 count, NET WT. 13.5, UPC 001960046003

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2310-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) BUTTERMILK 12 LOW FAT PANCAKES, NET WT14.5oz UPC 019600061007

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2294-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
Class IIModerate risk
FoodBacteria/virusRecalled May 5, 2017

AUNT JEMIMA(R) HOMESTYLE FRENCH TOAST, 6 COUNT, NET WT 12.5oz, UPC 019600057703

Potential for Listeria monocytogenes contamination

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
F-2300-2017
Lot/product code:
ALL
Recalling firm:
Pinnacle Foods, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled May 11, 2017

Sheridan SHER-I-SLIP and SOFT-TIP Intubating Stylets are intubating stylets manufactured from galvanized carbon steel and aluminum rods that are coated with a blue PVC or polypropylene outer covering and are designed to be placed inside an endotracheal tube to obtain a desired shape during intubation.

Product size listed on the labeling is incorrect.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77330
Lot/product code:
Product Code 5-15103 - Lot Number 73J1600218, 73K1600376, 73K1600587, 73L1600158, 73M1600275, 73A1700733;
Recalling firm:
Teleflex Medical
View official FDA record (opens in a new tab)
Class IIModerate risk
DrugRecalled May 16, 2017

Ventolin HFA (albuterol sulfate) Inhalation, 90 mcg per actuation, 200 Metered Inhalations, Net Wt. 18 g inhalers, Rx only, GlaxoSmithKline, Research Triangle Park, NC 27709, NDC 0173-0682-20.

Defective Delivery System: Elevated number of units with not meeting quality requirements results for leak rate

ALL 50 STATES
▸Full report

A moderate-risk recall. Using this product might cause temporary or reversible health problems, and serious harm is unlikely.

Recall #:
D-0793-2017
Lot/product code:
Lot#: 7ZP0634, 7ZP0810, 7ZP0990, Exp. 5/18
Recalling firm:
GlaxoSmithKline, LLC
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 2, 2017

Arctic Sun ArcticGel Pads - Medium, Product Code 317-07

Label on product box contains the incorrect reference #317-09 while the shelf box label with barcode and the internal foil pouch label are correctly labeled with product code 317-07 and lot number NDAR0462.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77469
Lot/product code:
Product code 317-07, Lot Number NGAR0462, Device Listing Number D234021.
Recalling firm:
C.R. Bard, Inc.
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 26, 2017

Cobalt MV with Gentamicin, Cobalt Bone Cement 40GM, REF 402439, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joint destruction following trauma or other conditions (also far fixation of unstable fractures in metastatic malignancies), and revision of previous arthroplasty procedures

Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77801
Lot/product code:
Lot Numbers: 508250, 959680
Recalling firm:
Encore Medical, Lp
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 26, 2017

Cobalt HV Bone Cement 40GM, REF 402282, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joint destruction following trauma or other conditions (also far fixation of unstable fractures in metastatic malignancies), and revision of previous arthroplasty procedures

Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77801
Lot/product code:
Lot Numbers: 508220, 189680, 199200, 310390, 424730, 668130, 668150, 871240, 959720
Recalling firm:
Encore Medical, Lp
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 26, 2017

Cobalt HV with Gentamicin, Cobalt Bone Cement 40GM, REF 402283, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joint destruction following trauma or other conditions (also far fixation of unstable fractures in metastatic malignancies), and revision of previous arthroplasty procedures

Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77801
Lot/product code:
Lot Numbers: 189690, 189760, 199180, 424740, 508240, 560290, 595660, 638280, 786630, 959650, 959700
Recalling firm:
Encore Medical, Lp
View official FDA record (opens in a new tab)
UnclassifiedRisk not yet known
Medical deviceRecalled June 26, 2017

Cobalt MV Bone Cement 40GM, REF 402438, QTY 1, STERILE, Rx Only, Mfgr: BIOMET ORTHOPEDICS Cobalt MV and HV Bone Cement is indicated for use as bone cement in arthroplastic procedures of the hip, knee and other joints to fix plastic and metal prosthetic parts to living bone when reconstructions is necessary because of osteoarthritis, rheumatoid arthritis, traumatic arthritis, avascular necrosis, nonunion of fractures of the neck of the femur, sickle cell anemia osteoporosis, secondary severe joint destruction following trauma or other conditions (also far fixation of unstable fractures in metastatic malignancies), and revision of previous arthroplasty procedures

Loss of the seal on the sterile Tyvek packaging used with this Cobalt Bone Cement.

ALL 50 STATES
▸Full report

FDA has not published a risk classification for this recall yet.

Recall #:
77801
Lot/product code:
Lot Numbers: 507830, 871270, 959670
Recalling firm:
Encore Medical, Lp
View official FDA record (opens in a new tab)