Search by meaning, not just keywords: describe the product or the hazard and we find matching recalls even when the official notice uses different words. Brand names and model numbers work too.
Latest recalls
35,004 found- Lower riskMedical device
Stryker Corporation recalls Spy-Phi Drape (HH2000) sold as a Spy-Phi Pack (HH9006). Only sold in the US. Drape/ UDI: HH2000/10858701006329; HH9006/
Stryker recalls Spy-Phi Drape (HH2000) and Spy-Phi Pack (HH9006) in the US due to sterile drapes packaged in unsealed pouches. Affected units have specific lot numbers.
StrykerJan 7, 2020 - Use cautionMedical device
CME America, LLC recalls CME America BodyGuard Infusion Pump System, All models of BG 323, BG 121, BG 545, BG CV545, BG 575, BG CV575, and
CME America recalls BodyGuard infusion pumps (BG 323, BG 121, etc.) due to potential 13% delivery inaccuracy at low/high flow rates. Affected units may deliver drugs too fast or too slow, risking treatment errors.
CME AmericaJan 7, 2020 - Use cautionMedical device
Smiths Medical ASD, Inc. recalls Portex ProVent Arterial Blood Sampling Kit with Dry Lithium Heparin for Gases and Electrolytes
Smiths Medical recalls Portex ProVent Arterial Blood Sampling Kits with dry lithium heparin for gases and electrolytes due to potential broken luer fittings. Affected units have specific lot numbers.
Smiths MedicalJan 7, 2020 - Use cautionMedical device
Palodex Group Oy recalls Instrumentarium Dental Express SOLID STATE X-RAY IMAGER (FLAT PANEL/DIGITAL IMAGER)
Instrumentarium recalls dental X-ray imagers with specific serial numbers due to potential short circuiting in the PSU that could cause heating, melting, and fire. Affected units have serial numbers starting with 1143, 1221, 1224, or 1229 followed by five digits.
Palod: InstrumentariumJan 7, 2020 - Lower riskMedical device
Zimmer Biomet, Inc. recalls THP Hip Plating System, Item Nos. 14-451070 14-451075 14-451080 14-451085 14-451090 14-451095 14-451100 14-451105
Zimmer Biomet recalls THP Hip Plating System with specific item numbers due to potential increased fracture rate and discoloration in packaging.
Zimmer BiometJan 7, 2020 - UnratedDrug
Preferred Pharmaceuticals, Inc recalls Preferred Pharmaceuticals, Inc, Ranitidine Tablets, 300 mg, Rx Only, a) 14 count bottles (NDC: 68788-6382-1), b) 30
Preferred Pharmaceuticals recalls ranitidine tablets due to NDMA impurity detected in product. This recall affects specific bottle sizes and lot numbers.
Preferred PharmaceuticalsJan 7, 2020 - UnratedDrug
Appco Pharma LLC recalls Ranitidine Capsules 300 mg, 30 count bottles. Rx only, Manufactured by: Appco Pharma LLC, Piscataway, NJ 08854,
Appco Pharma recalls 300mg Ranitidine Capsules due to potential NDMA impurity. Rx-only capsules manufactured in Piscataway, NJ with batch numbers 1905227UE and 1905228UE.
Appco PharmaJan 7, 2020 - Lower riskDrug
Mylan Pharmaceuticals Inc. recalls Nizatidine Capsules, USP 150 mg, Rx Only, Mylan Pharmaceuticals Inc., NDC 0378-5150-91.
Mylan recalls 150mg Nizatidine capsules due to trace NDMA impurity. This potential carcinogen may pose health risks. Consumers should check product details and follow official guidance.
MylanJan 7, 2020 - Lower riskDrug
Sigan Industries Inc. recalls Eczema Skin Relief Lotion, 2% Colloidal Oatmeal Skin Protectant Lotion, NET WT 14 OZ (396 g), NDC 65365-266-01,
Sigan Industries recalls 14 oz Eczema Skin Relief Lotion due to microbial contamination. Products distributed by CVS Pharmacy with specific lot numbers and expiration dates are affected. Consumers should check their product details and contact Sigan for guidance.
Sigan IndustriesJan 7, 2020 - UnratedDrug
AVKARE Inc. recalls Dutasteride Capsules, 0.5 mg, 30 Capsules (6 X 5) Unit Dose per carton, Rx Only, Manufactured for: AvKARE, Inc.,
AVKARE recalls Dutasteride Capsules (0.5 mg) due to high impurities that could cause harm. Affected lots expired by Feb 2021. Consumers should contact pharmacy for advice.
AVKAREJan 7, 2020 - Lower riskFood
ASK Foods Inc recalls ASK Foods Inc., KRAB SALAD, NET WT. 5 LB (2.27 kg), Plastic tub with a plastic lid,Keep Refrigerated, 2786-140
ASK Foods recalls KRAB SALAD (5 lb) due to potential metal pieces. Consumers should check product code 2786-140 and date code 2242.
ASK FoodsJan 7, 2020 - Lower riskFood
Attilio A Merlino and Associates Inc recalls Garbanzo Beans, Merlino Foods brand, sold in 5 lb. Polybag. No UPC.
Merlino Foods recalls 5-lb garbanzo beans from November 2019 to January 2020 due to potential glyphosate contamination. Consumers should check lot numbers 19318-19364 and 20006 for affected products.
Merlino FoodsJan 7, 2020 - Lower riskFood
Ingredion Incorporated recalls Ingredion ULTRA-TEX4 Food Starch in 50lb paper bags, product code 32166102CA
Ingredion recalls ULTRA-TEX4 Food Starch in 50lb paper bags (product code 32166102CA) due to potential stainless steel wire fragments that could cause injury.
IngredionJan 7, 2020 - Lower riskFood
Golden State Foods recalls Garlic Parmesan Sauce; DP# 4478 FG# 02620 8/16 fl. oz (4.73 ml) pouches; NET WT. 8.05 lbs (3.65 kg) Produced for
Golden State Foods recalls Garlic Parmesan Sauce pouches produced for Domino's Pizza due to metal fragments in starch ingredient used in manufacturing.
Golden State FoodsJan 7, 2020 - Use cautionVehicle
KEYSTONE SPRINGDALE (2020) recall — Suspension
Keystone is recalling 2020 Springdale trailers with incorrect 4400-pound axles and tires that could cause trailer overload and crash risk. Owners must replace parts by July 2020.
KeystoneJan 6, 2020 - Use cautionMedical device
Carestream Health, Inc. recalls Kodak DirectView DR3000/3500 - Product Usage: permanently installed as a diagnostic system intended to generate and
Carestream Health recalls Kodak DirectView DR3000 and DR3500 x-ray systems due to potential unintended movement of the U-Arm. Affected units have specific serial numbers. Consumers should contact Carestream for details.
Carestream HealthJan 6, 2020 - Use cautionMedical device
W. L. Gore & Associates Inc. recalls GORE¿ EXCLUDER¿ AAA Endoprosthesis
Gore recalls certain AAA endoprosthesis models due to reports of leading end catheter component separations. Affected products include specific catalog numbers and sizes. Consumers should contact Gore for details.
GoreJan 6, 2020 - Lower riskMedical device
Siemens Healthcare Diagnostics, Inc. recalls Atellica IM Humidity Pack (Qty 5), SMN 11313505, UDI 00630414234526, Software Version V1.21.0 and lower - Product
Siemens Healthcare recalls Atellica IM Humidity Packs with software version V1.21.0 or lower due to incorrect expiry ejection. Affected units may need replacement to prevent reagent analysis errors.
Siemens HealthcareJan 6, 2020 - Lower riskMedical device
MEDTECH SAS recalls ROSA Brain 3.0 Application-Brain
MEDTECH SAS recalls ROSA Brain 3.0 Application-Brain software with specific serial numbers due to potential image reconstruction errors that could compromise surgery planning. Affected units include 70 serial numbers listed in the recall notice.
MEDTECH SASJan 6, 2020 - Use cautionDrug
H J Harkins Company Inc dba Pharma Pac recalls Ranitidine, 150 mg Tablets, a) 7 count, b) 14 count, c) 20 count, d) 30 count, e) 60 count; Rx, Only, H.J. Harkins
H.J. Harkins recalls Ranitidine 150 mg tablets due to CGMP deviations and the presence of NDMA impurity. Check lot numbers RAN63KG through RAN66KG.
H.J. HarkinsJan 6, 2020 - Lower riskFood
Columbia Bean & Produce, Inc. recalls Dry Garbanzo Beans are sold under different brands and described as follows: -Bulk 2000 lbs. Totes. -CBP brand 25#
Columbia Bean & Produce recalls dry garbanzo beans with glyphosate levels exceeding safety limits. Products sold under CBP, FIESTA, Home Pride, and WinCo brands contain 11.8 ppm of glyphosate.
Columbia Bean & ProduceJan 6, 2020 - Lower riskFood
National Food & Beverage, Inc recalls Razzoo's Creole Sauce 10X4 LBS (1.8KG) Pouches Net Case Weight; 40 LBS STORE FROZEN
National Food & Beverage, Inc recalls Razzoo's Creole Sauce pouches due to undeclared codfish powder. Consumers should check best by dates and contact the company for details.
Razzoo'sJan 6, 2020 - Stop using nowFood
Lipari Foods Operating Company, LLC. recalls Premo and Fresh Grab Chicken Salad Wedge Sandwich, 5 oz., UPC: 612510002032
Lipari Foods recalls chicken salad sandwiches with potential Listeria monocytogenes contamination. Products with Best By date 2/6/20 or earlier are affected. Consumers should avoid these items.
Lipari FoodsJan 6, 2020 - Use cautionMeat & poultry
Kettle Cuisine Midco, LLC, Recalls Ready-To-Eat Soup Products due to Misbranding and Undeclared Allergens
USDA recalls Kettle Cuisine lentil and beef soup products due to undeclared egg and wheat allergens. Consumers urged to discard items purchased between Dec 2019 and Jan 2020.
Kettle CuisineJan 3, 2020 - UnratedMedical device
Pentax of America Inc recalls Pentax Video Colonoscope Model: EC38-i10L
Pentax recalls EC38-i10L colonoscopes sold without FDA approval. Affected units lack required safety clearance. Consumers should contact manufacturer for details.
PentaxJan 3, 2020 - Lower riskMedical device
Ethicon, Inc. recalls Coated VICRYL (Polyglactin 910) Suture, 18" (45cm) Product Code J497H. The device is a synthetic absorbable sterile
Ethicon recalls Coated VICRYL (Polyglactin : 18" sutures with lot number PGZ908 may have frayed sections that could reduce tensile strength during surgery.
EthiconJan 3, 2020 - Use cautionMedical device
Zimmer Surgical Inc recalls Zimmer Sterile Disposable Tourniquet Cuff with Protective Sleeve and PLC, Dual Port, Dual Bladder, Item No.
Zimmer recalls sterile disposable tourniquet cuffs with dual bladders due to potential leak causing both to inflate/deflate. Affected items have specific lot numbers and item codes.
ZimmerJan 3, 2020 - Lower riskMedical device
Microbiologics Inc recalls Vaginal Verification Panel Ref 8208 Lot 8208-11
Microbiologics recalls Vaginal Verification Panel Ref 8208 Lot 8208-11 due to Candida krusei contaminant in Pool 2. The recall explains the product's intended use for instrument verification and notes no impact on patient test results if Gardnerella vaginalis is properly detected.
MicrobiologicsJan 3, 2020 - UnratedMedical device
DePuy Orthopaedics, Inc. recalls SPECIALIST 2 DISTAL FEMORAL CUTTING BLOCK. Part code 966115. The product is a femoral cutting block.
DePuy recalls Specialist 2 Distal Femoral Cutting Blocks (part 966115) that won't connect to the Specialist 2 Locating Outrigger, making them unusable in surgery.
DePuyJan 3, 2020 - Lower riskMedical device
Bard Peripheral Vascular Inc recalls Bard Biopsy EnCor Probe, MRI, 10G Trocar Tip, REF number ECPMR0110G, packaged individually in sterile pouches, 5
Bard recalls MRI-compatible 10G trocar tips due to past probe failures causing leaks, suction problems, and sample collection issues. Affected units have specific lot numbers and packaging.
BardJan 3, 2020
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