Recalls affecting New Jersey

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

Recall #:

80533

Lot/product code:

7024260310

Recalling firm:

Withings Sas

A low-risk recall. This product is unlikely to cause any health problems, but it still doesn't meet FDA rules.

Recall #:

F-1592-2018

Lot/product code:

Lot #:160318-2 Exp: 03/2019, Lot# ASM4192017 Exp: 04-2020

Recalling firm:

Absonutrix

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

Recall #:

89584

Lot/product code:

All device serial numbers. Material Numbers 1040001 1054096 1054097 1054260 1054655 1058180 1119867 1040001B 1054096B 1054096NB 1054097B 1054260B 1054655B 1054655TP 1054655TPV 1058180B AU1054096 AU1054096B BR1054096 BT1054096 BT1054260 CA1054096 CA1054096B CN1054096 IT1054096B KO1054096 KR1054096 LA1054096 LG1054096 R1054096 R1054096B R1054097 R1054097B R1054260 R1054260B R1054655 R1054655B R1054655TP R1054655TPV R1119867 RSL1054260 RSL1054260B RTO1054260 RTO1054260B U1054096 U1054096B U1054097 U1054097B U1054260 U1054260B U1054655 RBR1054096 RTO1119867 1032800 1032802 1032804 1040002 1040005 1032800B 1032802B 1032804B 1032804TP 1032804TPV 1040002B 1040005B 1125564B AU1032800 AU1032800B BR1032800 CA1032800 CA1032800B IT1032800B KO1032800 KR1032800 LA1032800 LG1032800 R1032800 R1032802 R1032804 R1032804B R1032804TP R1032804TPV R1040005 R1040005B RTO1040005B SP1032800B U1032800 U1032802 U1032804 U1040005 U1040005B

Recalling firm:

Philips Respironics, Inc.

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

Recall #:

80313

Lot/product code:

All lots

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

80313

Lot/product code:

All lots

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

80313

Lot/product code:

All lots

Recalling firm:

Smith & Nephew, Inc.

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

Recall #:

80501

Lot/product code:

All Maestro 4000 Generators used with the optional foot switch.

Recalling firm:

Boston Scientific Corporation

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

Recall #:

82513

Lot/product code:

REBR1147, REBR1148, REBR1149, REBT0471, RECQ2162 and REBR1150

Recalling firm:

Bard Peripheral Vascular Inc

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

Recall #:

82662

Lot/product code:

Software Version 11.1

Recalling firm:

Elekta Instrument AB

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

Recall #:

85403

Lot/product code:

Device Model 550-000-000; UDI 00877972005230; Lot I8920/2020-08-29

Recalling firm:

Genicon, Inc.

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

Recall #:

82015

Lot/product code:

Device Identifier #: 08717648 01360 7 Part Number: 1000185 Lot number: 60047593

Recalling firm:

Abbott Vascular

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

Recall #:

D-0925-2018

Lot/product code:

Lot #: 7F021B, Exp 6/30/20

Recalling firm:

Sanofi-Aventis U.S. LLC

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

Recall #:

80717

Lot/product code:

2470 2480 2490 2501 2510 2521

Recalling firm:

Ortho Clinical Diagnostics Inc

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

Recall #:

81922

Lot/product code:

SmartStep Option

Recalling firm:

GE Healthcare, LLC

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

Recall #:

80717

Lot/product code:

2330 2340 2350 2360 2370 2380

Recalling firm:

Ortho Clinical Diagnostics Inc

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

Recall #:

80717

Lot/product code:

5535 5540 5550 5560 5570 5580 5590 5600 5610 5615 5620 5630 5640 5650 5655 5660 5665 5670 5675 5678 5680 5685 5690

Recalling firm:

Ortho Clinical Diagnostics Inc

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

Recall #:

80717

Lot/product code:

2470 2480 2490 2500 2510 2520 2530

Recalling firm:

Ortho Clinical Diagnostics Inc

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

Recall #:

D-0970-2018

Lot/product code:

All lots within expiry.

Recalling firm:

Prinston Pharmaceutical Inc

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

Recall #:

D-0972-2018

Lot/product code:

All lots within expiry.

Recalling firm:

Prinston Pharmaceutical Inc

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

Recall #:

80645

Lot/product code:

UDI# VS4 (863283): 00884838087095

Recalling firm:

Philips Electronics North America Corporation

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

Recall #:

D-0969-2018

Lot/product code:

All lots within expiry.

Recalling firm:

Prinston Pharmaceutical Inc

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

Recall #:

D-0975-2018

Lot/product code:

All lots within expiry.

Recalling firm:

Prinston Pharmaceutical Inc

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

Recall #:

D-0971-2018

Lot/product code:

All lots within expiry.

Recalling firm:

Prinston Pharmaceutical Inc

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

Recall #:

80645

Lot/product code:

UDI# VS2 (863079): 00884838009639, (863080): 00884838009646, (863081): 00884838009653, (863082): 00884838009660

Recalling firm:

Philips Electronics North America Corporation

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

Recall #:

80645

Lot/product code:

UDI# VS3 (863069): 00884838000094, (863070): 00884838000100, (863071): 00884838000117, (863072): 00884838000124, (863073): 00884838000131, (863074): 00884838000148

Recalling firm:

Philips Electronics North America Corporation