Product Recalls in Pennsylvania
Product recalls affecting Pennsylvania — including food, drugs, consumer products, medical devices, and vehicles distributed to Pennsylvania. RecallDetector monitors distribution data from the FDA, USDA, CPSC, and NHTSA to show you which recalls are relevant to your area. 1,064 recalls have been distributed to Pennsylvania in the last 12 months.
Showing 21701–21720 of 55,602 recalls
Recalled Item: VitreQ 23G Silicone Tipped Cannula-CN23.D01 GTIN: 8719214221508 Recalled by...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: VitreQ 23G PFC Injection Needle- .D01 GTIN: 8719214221362 Recalled by Vitreq...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: (1) VitreQ 23G BF Blunt Needles-BF23.D51 GTIN#: 8719214221126 (2) VitreQ...
The Issue: Microscopic tears of the sterile pouch may compromise sterility
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Arthrex Fibulock Fibular Nail Instrument Set Reusable non-sterile...
The Issue: There is a potential for blockage of the Hub Attachment Tube.
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Recalled by Quest Medical, Inc. Due to Additive and Arrest Agent Labels on...
The Issue: Additive and Arrest Agent Labels on the MPS Top Cover Replacement Kit, a...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: AMS 700 100 mL Recalled by Boston Scientific Corporation Due to A labeling...
The Issue: A labeling discrepancy incorrectly labeled AMS 700 100mL Conceal Low Profile...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: GREY GHOST BAKERY scratch-made cookies LEMON SUGAR NET WT 1.4 OZ (40 G)...
The Issue: The product contains undeclared sulfites.
Recommended Action: Do not consume. Return to store for a refund or discard.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Ketorolac Tromethamine Injection Recalled by Hikma Pharmaceuticals USA Inc....
The Issue: Presence of Particulate Matter: particles identified as polydimethylsiloxane...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Hydrocortisone and Acetic Acid Otic Solution Recalled by Akorn Inc Due to...
The Issue: Subpotent Drug: Low Out of specification (OOS) assay results for the...
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 500 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 8 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: NORepinephrine Bitartrate 4 mg added to 250 mL 5% Dextrose Recalled by...
The Issue: Subpotent Drug
Recommended Action: Stop taking this medication. Contact your pharmacy or healthcare provider.
Recalled Item: Centricity Universal Viewer 6.0 Recalled by GE Healthcare, LLC Due to...
The Issue: Centricity Universal Viewer measurements saved into a DICOM Grayscale...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 24MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: LEGION AP Cutting Block Size 4 Recalled by Smith & Nephew, Inc. Due to...
The Issue: Multiple lots of LEGION AP Femoral Cutting Blocks were manufactured with an...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 16MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 12MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: Microbiologics QC Sets and Panels Recalled by Microbiologics Inc Due to The...
The Issue: The recommended hydration fluid for the 8180 Gram-Positive Blood Culture...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.
Recalled Item: 2.4MM TI VA LOCKING SCREW STARDRIVE 18MM STERILE Recalled by Synthes, Inc....
The Issue: There is a possibility that the inner cap could open when the outer cap is...
Recommended Action: Stop using. Contact the manufacturer or your healthcare provider.