Product Recalls in New Jersey

Product recalls affecting New Jersey — including food, drugs, consumer products, medical devices, and vehicles distributed to New Jersey. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 2,841 recalls have been distributed to New Jersey in the last 12 months.

53,621 total recalls
2,841 in last 12 months

Showing 52415260 of 53,621 recalls

Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Match Head Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 24, 2024· Stryker Corporation

Recalled Item: Stryker iBur 3.0mm Diamond Round Recalled by Stryker Corporation Due to...

The Issue: Potential for the product to exhibit temperatures higher than specification...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 24, 2024· B. Braun Medical Inc

Recalled Item: 0.9% Sodium Chloride Injection USP Recalled by B. Braun Medical Inc Due to...

The Issue: Presence of Particulate Matter

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class I — Serious Health HazardOngoing
Refund
DrugJuly 23, 2024· FDC Limited

Recalled Item: Ciprofloxacin ophthalmic solution USP Recalled by FDC Limited Due to...

The Issue: Defective container: unable to get the solution out of the bottle as the...

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Unomedical A/S

Recalled Item: VariSoft Infusion Set Recalled by Unomedical A/S Due to Specific VariSoftTM...

The Issue: Specific VariSoftTM Infusion Sets were packaged using incorrect secondary...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 23, 2024· Karl Storz Endoscopy

Recalled Item: Karl Storz - Endoskope Recalled by Karl Storz Endoscopy Due to Various...

The Issue: Various medical device product IFUs contain reprocessing modalities that...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
DrugJuly 22, 2024· Glenmark Pharmaceuticals Inc., USA

Recalled Item: Glenmark Recalled by Glenmark Pharmaceuticals Inc., USA Due to CGMP Deviations

The Issue: CGMP Deviations

Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 20, 2024· Izzio Artisan Bakery, LLC

Recalled Item: Izzio Everything Sourdough. Single 24oz loaf packaged into plastic bag....

The Issue: Potential foreign material - plastic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 20, 2024· Izzio Artisan Bakery, LLC

Recalled Item: Izzio Everything Roll packaged in 12oz plastic bag Recalled by Izzio Artisan...

The Issue: Potential foreign material - plastic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
FoodJuly 20, 2024· Izzio Artisan Bakery, LLC

Recalled Item: Aldi Mixed Sourdough loaf. A single 24oz loaf packaged into plastic bag...

The Issue: Potential foreign material - plastic

Recommended Action: Do not consume. Return to store for a refund or discard.

Class II — Potential Health HazardOngoing
Refund
Medical DeviceJuly 19, 2024· Inari Medical - Oak Canyon

Recalled Item: ClotTriever XL Catheter Recalled by Inari Medical - Oak Canyon Due to...

The Issue: Thrombectomy system catheter instructions for use updated to reduce adverse...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class I — Serious Health HazardOngoing
Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing
Medical DeviceJuly 18, 2024· Centinel Spine, Inc.

Recalled Item: prodisc C SK Recalled by Centinel Spine, Inc. Due to During the assembly of...

The Issue: During the assembly of Prodisc C, a blue discoloration was observed on a...

Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.

Class II — Potential Health HazardOngoing