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. 1,120 recalls have been distributed to New Jersey in the last 12 months.
Showing 11621–11640 of 53,621 recalls
Recalled Item: Surgipro II Monofilament Polypropylene Sutures Product Description Model...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Sofsilk Coated Braided Silk Suture Product Description CS-211 SOFSILK* 4-0...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Monosof Monofilament Nylon sutures: Product Description CN-724 MONOSOF* 1...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgidac Uncoated Braided Polyester suture Product Description D-1764K...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Codman Surgical Patties Recalled by Integra LifeSciences Corp. Due to...
The Issue: Integra LifeSciences identified that one lot was released with...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Lamaze Chill Teether Recalled by Tomy International Inc. Due to Affected...
The Issue: Affected lots of the product are being recalled due to potential microbial...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgilon Braided Nylon suture Product Description: 88861883-51 SURGILON* 2-0...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Surgipro Monofilament Polypropylene Sutures Product Description CP-535...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Novafil Monofilament Polybutester Suture Product Description: 8886 4002-41...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Custom Suture Pack Product Description: US1638 CUSTOM SUTURE PACK US1756...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dermalon Monofilament Nylon Suture: (1) 88861741-11 DERMALON* 6-0 BLU 45CM...
The Issue: Sterile Barrier Breach of Breather Pouch may cause infection or vision loss...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Oxcarbazepine Tablets 600mg Recalled by SUN PHARMACEUTICAL INDUSTRIES INC...
The Issue: Presence of foreign substance
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Premium Quality Shirakiku Fish Sausage Original Net wt. 9.8 oz. Recalled by...
The Issue: Undeclared collagen (bovine dermis) casing
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Premium Quality Shirakiku Fish Sausage Jalapeno Net wt. 9.8 oz. Recalled by...
The Issue: Undeclared collagen (bovine dermis) casing
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Beaver EdgeAhead Stiletto/MVR Knife .90mm Straight (20G)-for ocular...
The Issue: Packaging sterile barrier has been compromised. Open seals can lead to a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ActiveAid 922 Recalled by Altimate Medical, Inc. Due to Device manufactured...
The Issue: Device manufactured with a component with affects the foldability of the...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Source Administration Set (SAS) used with the Medrad Intego PET Infusion...
The Issue: Black specks may be present on the packaged needles
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dual-Trak Clavicle Screws Part Number/Part Description: 40-0136 3.0mm x 80mm...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AcuTwist Acutrak Compression Screws Part Number/Part Description: AI-0010-S...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Part Number/Part Description: 30-0033-S 30mm Acutrak¿ Fusion Device 6mm Nose...
The Issue: Distribution without Pre-Market Clearance
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.