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. 1,777 recalls have been distributed to New Jersey in the last 12 months.
Showing 48481–48500 of 53,621 recalls
Recalled Item: Introvale (levonorgestrel and ethinyl estradiol) tablets Recalled by Sandoz...
The Issue: Contraceptive tablets out of sequence: Contraceptive tablets out of...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: E-Z Clean¿ Disposable Laparoscopic Electrode Model Number 0100L and 0100LS....
The Issue: Megadyne Medical Products is recalling certain lots of E-Z Clean, L-Wire...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Ultrasound ViewPoint 6. Product Usage: ViewPoint is intended to Recalled...
The Issue: GE has recently become aware of a potential safety issue due to the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Philips MR Systems: Asset 0.5T Recalled by Philips Medical Systems...
The Issue: There is a potential for water to collect in the vent pipe elbow in the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Enhancement Medical expression. model # EXP-150. Injectable Gel 1.5cc...
The Issue: Manufacturer made a change in the production process that resulted in a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefibre Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Benefiber Recalled by Novartis Consumer Health Due to The lot number and/or...
The Issue: The lot number and/or expiration date may be illegible on the outer plastic...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.3 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture Recalled...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: BIORAPTOR 2.9 mm Suture Anchor Straight Recalled by Smith & Nephew, Inc....
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX Ultra 5.5 mm PLLA-HA Suture Anchor with two #2 ULTRABRAID Sutures...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR 2.9 mm Suture Anchor with 2 ULTRABRAID Suture Recalled by Smith...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTEORAPTOR CURVED 2.3 mm Suture Anchor SA ULTRABRAID COBRAID Suture...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX" Ultra PLLA/HA 6.5 mm with 2 ULTRABRAID" Suture Recalled by Smith &...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: OSTOSTEORAPTOR 2.9 mm Suture Anchor with 1 ULTRABRAID COBRAID Suture...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TWINFIX ULTRA PLLA/HA 5.5 mm Suture Anchor with 3 ULTRABRAID Recalled by...
The Issue: Pinholes detected in a small number of primary pouches that may constitute a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.