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. 2,642 recalls have been distributed to New Jersey in the last 12 months.
Showing 27421–27440 of 29,496 recalls
Recalled Item: LPC Fine Mesh Cassette for the Leica LPC Printer. Part No: 14060546848...
The Issue: An LPC Fine Mesh Cassette failed to stay closed during processing operations.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Cobas¿ 8000 modular analyzer series software version 03-01 Recalled by Roche...
The Issue: When using the cobas e 602 module, Diluent Multiassay may be used for...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Software correction applies to customers who use the RT Therapist Recalled...
The Issue: Software update to fix multiple safety related issues.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: ExoShape Soft Tissue Fastener 12 mm x 30 mm by Medshape Solutions, INC. Due...
The Issue: Expiration date on the patient label and date on the product carton were not...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: PTS PANELS Recalled by Polymer Technology Systems, Inc. Due to Internal...
The Issue: Internal investigation demonstrated under-recovery for glucose when tested...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: remel RapID Yeast Plus System Recalled by Remel Inc Due to Mislabeling
The Issue: The two reagents supplied in the RapID Yeast Plus System kit (Reagent A and...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 20mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 13mm addEASE(TM) Binary Connector with 17 Ga. Needle for use Recalled by B....
The Issue: Possible solution leakage at the interface of the addEASE(TM) Binary...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosure Ratchet Driver Recalled by Smith & Nephew, Inc., Endoscopy Div. Due...
The Issue: Driver does not meet specification, oversized. Driver may not be able to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Biosure Driver Recalled by Smith & Nephew, Inc., Endoscopy Div. Due to...
The Issue: Driver does not meet specification, oversized. Driver may not be able to be...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: TOSHIBA Kalare Diagnostic X-Ray System K110785 Recalled by Toshiba American...
The Issue: Firm initiated recall because when radiographic conditions with the small...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: SOLAR 8000 AND TRANSPORT PRO WITH PATIENT DATA MODULE (Marketed Recalled by...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GE Healthcare Recalled by GE Healthcare, LLC Due to GE Healthcare has...
The Issue: GE Healthcare has recently become aware of a potential safety issue due to...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VITROS Immunodiagnostic Products CK-MB Calibrators Recalled by...
The Issue: Internal testing demonstrated that opened-reconstituted VITROS CK-MB...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Product is distributed by Zimmer (Warsaw Recalled by Synvasive Technology...
The Issue: Various reciprocating and oscillating saw blades were incorrectly labeled....
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14219-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14210-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2008 MeDS Pump Recalled by Fresenius Medical Care Holdings, Inc. dba Renal...
The Issue: Product is being recalled because the combination of the current 50 mg vial,...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: List No. 14203-28 Recalled by Hospira Inc. Due to It was discovered that...
The Issue: It was discovered that there was a potential for the piercing pin on certain...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.