989 recalls tagged with “adult product”.
StopBox USA recalls AR-15 Chamber Lock Pro shipped June 2 to July 15, 2025. The recall covers locks designed to chamber-lock AR-15 style rifles. The defect allows the lock to be forcibly removed, enabling unauthorized access to the firearm. StopBox urges immediate stop-use and provides refunds or replacements.
Organicare Nature's Science recalled 15,075 bottles of FemiClear Daily Bladder Strength, sold in retail stores across all 50 states and Puerto Rico and online. The recall cites microbial contamination with Escherichia coli O7:K1 and E. coli 1303. Consumers should stop using the product and contact Organicare Nature's Science for a refund or replacement.
American Contract Systems recalled 32,433 radiology packs after a nonconformance during EO gas injection. The items were re-gassed and not validated for multiple sterilization cycles. The recall is active as of 2025-10-22. US distribution included SD, IA, MN, WA, IL. Health risks prompt immediate removal from use.
Gospodarstwo Pasieczne Sadecki Bartnik recalled 336 jars of Bee Pollen sold in Illinois after tests detected pyrrolizidine alkaloids. The product contains detectable pyrrolizidine alkaloids. Consumers should not consume the product and should contact the producer by telephone for refund or replacement.
American Contract Systems Inc. recalls 32,433 medical convenience kits distributed nationwide to healthcare facilities in SD, IA, MN, WA, and IL. Re-gassed after a nonconformance occurred during Ethylene Oxide gas injection. The kits have not been validated for multiple sterilization cycles. Healthcare providers should stop using the devices immediately and follow recall instructions.
American Contract Systems recalled 32,433 medical convenience kits nationwide in the United States after re-gassing sterilization cycles. The recall covers multiple packs including HEART PACK and PACEMAKER PACK with 2025 recall date. The safety issue centers on EO gasset validation failures after a nonconformance during initial gas injection. Stop using immediately and follow recall instructions.
Pacific Coast Producers recalled 203 cases of Pears Sliced in Organic Pear Juice from Concentrate distributed by Wegmans Food Markets. The products may be contaminated with lead. Consumers should not eat them and should contact Pacific Coast Producers by telephone for refund or replacement.
American Contract Systems recalled 32,433 medical convenience kits nationwide after finding re-gassed devices from EO sterilization. The recall affects five product lines with UDI-DI codes and Lot numbers. The re-gassing process has not been validated for multiple sterilization cycles, calling into question product safety and effectiveness. Health providers and patients should stop using these kit
American Contract Systems recalled 32,433 medical convenience kits sold through multiple retailers nationwide. The devices were re-gassed after a nonconformance in the Ethylene Oxide gas injection process and have not been validated for exposure to multiple sterilization cycles. Healthcare providers and patients should stop using these products immediately and follow the manufacturer's recall.
Zydus Lifesciences Ltd. recalled Chlorpromazine Hydrochloride tablets, 25 mg, 100-count bottles distributed nationwide by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ 08534. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc. for
Zydus Lifesciences and Zydus Pharmaceuticals US recall Chlorpromazine Hydrochloride Tablets, 10 mg, 100-count bottles sold nationwide in the United States after detecting an impurity above acceptable intake. The impurity is N-Nitroso Desmethyl Chlorpromazine. Consumers should stop using the product immediately and contact the manufacturer for guidance.
Philips Medical Systems Nederland recalled 174 Allura Xper FD20 OR Tables worldwide, including 45 in the United States. The devices may deteriorate internally, rendering motorized movements inoperable. Hospitals and clinics should stop using the devices and follow the manufacturer's recall instructions.
Philips Medical Systems Nederland B.V. recalls 98 imaging systems worldwide after reports of component deterioration. Systems may lose motorized movements due to CMOS battery, hard disk drive, or power supply deterioration. Imaging remains available. Stop using the device and follow manufacturer instructions.
Philips Medical Systems Netherlands B.V. recalled 3 Allura Xper FD20/20 OR Tables worldwide, including the US, on 2025-09-03 after detection of degradation in internal components. The recall cites CMOS battery, hard disk drive, and/or power supply unit deterioration. Motorized movements may fail while imaging remains available. The recall is active. Stop using the device following recall guidance.
Zydus Lifesciences Chlorpromazine Hydrochloride Tablets, 100 mg, 100-count bottles distributed nationwide in the USA for Northstar Rx LLC, Memphis, TN 38141, are recalled. The recall cites CGMP deviations with the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake. Healthcare providers and patients should stop using the product immediately and contact the manufacturer or a医
Zydus Lifesciences and Northstar Rx LLC recall Chlorpromazine Hydrochloride Tablets, 50 mg, 100-count bottles distributed nationwide in the United States. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. Stop using the product immediately and contact your healthcare provider or Zydus Pharmaceuticals (USA) Inc for guidance.
Zydus Lifesciences Ltd. recalled chlorpromazine hydrochloride tablets nationwide in the United States after tests found N-Nitroso Desmethyl Chlorpromazine above the acceptable intake limit. The issue involves CGMP deviations in manufacturing at the India facility and distribution by Zydus Pharmaceuticals (USA) Inc., Pennington, NJ. Healthcare providers and patients should stop using the product, 0
Endico Potatoes Inc. recalled 335 cases of Endico brand PEAS & CARROTS distributed to seven states after authorities flagged Listeria monocytogenes. The product should not be eaten. Consumers should contact Endico Potatoes for refund or replacement information. The recall was active as of Sept. 3, 2025.
The FDA confirms a nationwide recall of Zydus Lifesciences Chlorpromazine Hydrochloride tablets 200 mg (NDC 70710-1133-1) distributed by Zydus Pharmaceuticals USA. The recall cites CGMP deviations and the presence of N-Nitroso Desmethyl Chlorpromazine above acceptable intake. Consumers and healthcare providers should stop using the product immediately and contact the distributor for guidance.
Chlorpromazine Hydrochloride Tablets, 200 mg, 100-count bottle, manufactured by Zydus Lifesciences Ltd. and distributed by Northstar Rx LLC, are under recall nationwide in the United States. The CGMP deviation involves elevated levels of N-Nitroso Desmethyl Chlorpromazine. Consumers should stop use and contact their healthcare provider.