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. 2,639 recalls have been distributed to New Jersey in the last 12 months.
Showing 32701–32720 of 53,621 recalls
Recalled Item: Estradiol Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical, Co....
The Issue: cGMP Deviations; lack of quality assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ethinyl Estradiol Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...
The Issue: cGMP Deviations; lack of quality assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Levonorgestrel Non-Micronized Recalled by Qinhuangdao Zizhu Pharmaceutical,...
The Issue: cGMP Deviations; lack of quality assurance.
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Craftmatic Model 1 Base for Dual Bed Configurations Recalled by Craftmatic...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Legacy Base for Dual Bed Configurations Recalled by Craftmatic Industries,...
The Issue: A potential for dual-configured beds to separate or slip away from one another.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: WECK Visistat 35R Disposable Skin Stapler Recalled by Teleflex Medical Due...
The Issue: Some boxes are labeled as containing Visistat Wide devices, when they in...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio-SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with BioComposite SwiveLock SP Vented...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex PEEK SwiveLock SP Vented Recalled by Arthrex, Inc. Due to Some...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex Bio Composite SwiveLock SP Vented Recalled by Arthrex, Inc. Due to...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Anthrex SpeedBridge Implant System with PEEK SwiveLock Self Punching...
The Issue: Some eyelets broke from SwiveLock Anchor on insertion.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Adhesive Base Product # 273 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Dale Medical Stabilock Endotracheal Tube Holder Product # 270 The Recalled...
The Issue: ET Tube Holders contain an adhesive faceplate that may lose its adhesive...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Blood Agar (TSA w/ 5% Sheep Blood) Plate Recalled by Remel Inc Due to...
The Issue: Confirmed complaint of surface contamination of Listeria monocytogenes.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: MP MUSCLEPHARM Recalled by Armada Nutrition Due to A raw material initially...
The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Muscle Meds(TM) PERFORMANCE TECHNOLOGIES Recalled by Armada Nutrition Due to...
The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: MYPROTEIN Recalled by Armada Nutrition Due to A raw material initially...
The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: USN B4 -BOMB EXTREME PRE-WORKOUT Recalled by Armada Nutrition Due to A raw...
The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: BULK PRODUCT: MYPROTEIN Recalled by Armada Nutrition Due to A raw material...
The Issue: A raw material initially failed testing Staphylococcus aureus. A retest was...
Recommended Action: Do not consume. Return to store for a refund or discard.